03.06.2024 | Full-time | PharmiwebClinical Research Associate IQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebRelated problems and prioritize workload for self and team You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). Fluent Romanian and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebRelated problems and prioritize workload for self and team You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). Fluent Romanian and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | Craiova | PharmiwebRelated problems and prioritize workload for self and team You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). Fluent Romanian and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
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